Neutral Sphingomyelinase 2 (SMPD3) Deficiency in Mice Causes Chondrodysplasia with Unimpaired Skeletal Mineralization-Reference-Cited by-同舟云学术

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Neutral Sphingomyelinase 2 (SMPD3) Deficiency in Mice Causes Chondrodysplasia with Unimpaired Skeletal Mineralization

Published:2019-09 Issue:9 Volume:189 Page:1831-1845
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Stoffel Wilhelm,Hammels Ina,Jenke Britta,Schmidt-Soltau Inga,Niehoff Anja

Funder

Centre of Molecular Medicine Cologne

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference29 articles.

1. The ceramide-centric universe of lipid-mediated cell regulation: stress encounters of the lipid kind;Hannun;J Biol Chem,2002

2. Cloned mammalian neutral sphingomyelinase: functions in sphingolipid signaling?;Tomiuk;Proc Natl Acad Sci U S A,1998

3. Cloning and characterization of the mammalian brain-specific, Mg2+-dependent neutral sphingomyelinase;Hofmann;Proc Natl Acad Sci U S A,2000

4. Identification and characterization of murine mitochondria-associated neutral sphingomyelinase (MA-nSMase), the mammalian sphingomyelin phosphodiesterase 5;Wu;J Biol Chem,2010

5. Reply to kolesnick and hannun, and perry and hannun;Hofmann;Trends Biochem Sci,1999

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